Immunophenotype and functional properties of feline dendritic cells derived from blood and bone marrow

被引:38
作者
Bienzle, D [1 ]
Reggeti, F [1 ]
Clark, ME [1 ]
Chow, C [1 ]
机构
[1] Univ Guelph, Dept Pathobiol, Guelph, ON N1G 2W1, Canada
关键词
cat; immunity; antigen-presenting cells; bone marrow culture; MHC CLASS-II; COMPLEX CLASS-II; IN-VITRO; MANNOSE RECEPTOR; ANTIGEN; DIFFERENTIATION; MACROPHAGES; CD1; PHAGOCYTOSIS; EXPRESSION;
D O I
10.1016/S0165-2427(03)00132-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are a heterogeneous population of cells of fundamental importance in initiating innate as well as specific immune responses. The identity and function of DCs in the cat are unknown, although they are likely pivotal in the response to infection. In this study. feline DCs were derived by 3-10-day culture of adherent blood mononuclear cells (PBMCs) and bone marrow mononuclear cells (BMMCs) in the presence of IL 4 and GM-CSF. BMMC consistently yielded a greater number of DCs than PBMC. and there were fewer macrophages than DC from both compartments. DCs expressed a distinct constellation of surface molecules, which included CD1a, CD1b, and CD1c, CD11b, CD14, and 2-3-fold higher levels of MHC class I and II molecules than co-cultured macrophages or fresh blood monocytes. DCs displayed typical cytoplasmic processes, limited nonspecific esterase activity, and acquired antigen by phagocytosis, pinocytosis, and binding to specific receptors. Cytokine-exposed cells induced proliferation of allogeneic lymphocytes. Thus, the cells derived by these culture conditions had markers and functions analogous to immature myeloid DCs. Availability of feline DCs will enable investigation of their role in infectious disease and their potential therapeutic application. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 30
页数:12
相关论文
共 48 条
  • [1] BIENZLE D, 2001, SCHALMS VET HEMATOLO, P318
  • [2] Generation of phagocytic MAK and MAC-DC for therapeutic use: Characterization and in vitro functional properties
    Boyer, A
    Andreu, G
    Romet-Lemonne, JL
    Fridman, WH
    Teillaud, JL
    [J]. EXPERIMENTAL HEMATOLOGY, 1999, 27 (04) : 751 - 761
  • [3] INFECTION OF PERITONEAL-MACROPHAGES INVITRO AND INVIVO WITH FELINE IMMUNODEFICIENCY VIRUS
    BRUNNER, D
    PEDERSEN, NC
    [J]. JOURNAL OF VIROLOGY, 1989, 63 (12) : 5483 - 5488
  • [4] IL-4 and CD40 ligation affect differently the differentiation, maturation, and function of human CD34+ cell-derived CD1a+CD14- and CD1a-CD14+ dendritic cell precursors in vitro
    Canque, B
    Camus, S
    Yagello, M
    Gluckman, JC
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 64 (02) : 235 - 244
  • [5] CD1 molecules efficiently present antigen in immature dendritic cells and traffic independently of MHC class II during dendritic cell maturation
    Cao, XC
    Sugita, M
    van der Wel, N
    Lai, J
    Rogers, RA
    Peters, PJ
    Brenner, MB
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 169 (09) : 4770 - 4777
  • [6] Porcine dendritic cells generated in vitro:: morphological, phenotypic and functional properties
    Carrasco, CP
    Rigden, RC
    Schaffner, R
    Gerber, H
    Neuhaus, V
    Inumaru, S
    Takamatsu, H
    Bertoni, G
    McCullough, KC
    Summerfield, A
    [J]. IMMUNOLOGY, 2001, 104 (02) : 175 - 184
  • [7] Generation of blood-derived dendritic cells in dogs with oral malignant melanoma
    Catchpole, B
    Stell, AJ
    Dobson, JM
    [J]. JOURNAL OF COMPARATIVE PATHOLOGY, 2002, 126 (2-3) : 238 - 241
  • [8] Distinct mRNA microarray profiles of tolerogenic dendritic cells
    Cortesini, NSF
    Piazza, F
    Ho, E
    Ciubotariu, R
    LeMaoult, J
    Dalla-Favera, R
    Cortesini, R
    [J]. HUMAN IMMUNOLOGY, 2001, 62 (10) : 1065 - 1072
  • [9] ISOLATION AND FUNCTIONAL-STUDIES ON FELINE BONE-MARROW DERIVED MACROPHAGES
    DANIEL, SL
    LEGENDRE, AM
    MOORE, RN
    ROUSE, BT
    [J]. VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1993, 36 (02) : 107 - 122
  • [10] Naked antigen-presenting molecules on dendritic cells
    Davoust, J
    Banchereau, J
    [J]. NATURE CELL BIOLOGY, 2000, 2 (03) : E46 - E48